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dc.contributor.authorXu, Jianwen
dc.contributor.authorPrifti, Fioleda
dc.contributor.authorSong, Jie
dc.date2022-08-11T08:10:09.000
dc.date.accessioned2022-08-23T16:57:09Z
dc.date.available2022-08-23T16:57:09Z
dc.date.issued2011-04-26
dc.date.submitted2012-01-24
dc.identifier.citationMacromolecules. 2011 Apr 26;44(8):2660-2667. <a href="http://dx.doi.org/10.1021/ma200021m">Link to article on publisher's site</a>
dc.identifier.issn0024-9297 (Linking)
dc.identifier.doi10.1021/ma200021m
dc.identifier.pmid21686053
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43080
dc.description.abstractDespite the increasing demands for functional degradable biomaterials, strategies for generating materials with modular compositions and well-defined functionalities from common building blocks are still lacking. Here we report an azido-functionalized cyclic carbonate monomer, AzDXO, that exhibited controlled/"living" ring-opening polymerization kinetics under the catalysis of 1,8-diazabicyclo[5.4.0]-undec-7-ene. Homopolymerization of AzDXO and copolymerization of AzDXO with lactide resulted in polycarbonate and poly(ester-carbonates) with well-defined composition and narrow polydispersity. Further side-chain functionalizations of these polymers were accomplished under facile conditions via copper-catalyzed or copper-free strain-promoted azido-alkyne cyclcoaddition. This versatile monomer building block, obtainable in two steps without tedious purifications, provides a practical solution to the preparation of well-defined functional polycarbonates and poly(ester-carbonates).
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=21686053&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1021/ma200021m
dc.subjectBiocompatible Materials
dc.subjectBiomaterials
dc.subjectOrthopedics
dc.subjectRehabilitation and Therapy
dc.titleA Versatile Monomer for Preparing Well-Defined Functional Polycarbonates and Poly(ester-carbonates)
dc.typeJournal Article
dc.source.journaltitleMacromolecules
dc.source.volume44
dc.source.issue8
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/ortho_pp/93
dc.identifier.contextkey2468294
html.description.abstract<p>Despite the increasing demands for functional degradable biomaterials, strategies for generating materials with modular compositions and well-defined functionalities from common building blocks are still lacking. Here we report an azido-functionalized cyclic carbonate monomer, AzDXO, that exhibited controlled/"living" ring-opening polymerization kinetics under the catalysis of 1,8-diazabicyclo[5.4.0]-undec-7-ene. Homopolymerization of AzDXO and copolymerization of AzDXO with lactide resulted in polycarbonate and poly(ester-carbonates) with well-defined composition and narrow polydispersity. Further side-chain functionalizations of these polymers were accomplished under facile conditions via copper-catalyzed or copper-free strain-promoted azido-alkyne cyclcoaddition. This versatile monomer building block, obtainable in two steps without tedious purifications, provides a practical solution to the preparation of well-defined functional polycarbonates and poly(ester-carbonates).</p>
dc.identifier.submissionpathortho_pp/93
dc.contributor.departmentDepartment of Cell Biology
dc.contributor.departmentDepartment of Orthopedics and Physical Rehabilitation
dc.source.pages2660-2667


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